Hasil Pencarian - Mohammad KERAMATIPOUR

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  1. 1
    Identification of a Novel Mutation in CNNM4 Gene in an Iranian Family with Jalili Syndrome

    Identification of a Novel Mutation in CNNM4 Gene in an Iranian Family with Jalili Syndrome oleh Mohammad Ghofrani, Mohammad Keramatipour

    Diterbitkan 2019-10-01
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  2. 2
    Effect of Embryonic Cerebrospinal Fluid on Proliferation and Differentiation of Neuroprogenitor Cells

    Effect of Embryonic Cerebrospinal Fluid on Proliferation and Differentiation of Neuroprogenitor Cells oleh Mohammad Keramatipour, Mohammad Nabiuni, Kazem Parivar, Siamak Yari

    Diterbitkan 2013-01-01
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  3. 3
    Lack of Association between Single Nucleotide Polymorphism rs10818488 in TRAF1/C5 Region and Rheumatoid Arthritis in Iranian Population

    Lack of Association between Single Nucleotide Polymorphism rs10818488 in TRAF1/C5 Region and Rheumatoid Arthritis in Iranian Population oleh Somayeh Ahmadlou, Mohsen Akhiani, Ahmad Salimzadeh, Mohammad Keramatipour

    Diterbitkan 2014-02-01
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  4. 4
    SPOAN syndrome: a novel mutation and new ocular findings; a case report

    SPOAN syndrome: a novel mutation and new ocular findings; a case report oleh Fatemeh Bazvand, Mohammad Keramatipour, Hamid Riazi-Esfahani, Alireza Mahmoudi

    Diterbitkan 2021-01-01
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  5. 5
    Comparison of Two Different PCR-based Methods for Detection of GAA Expansions in Frataxin Gene

    Comparison of Two Different PCR-based Methods for Detection of GAA Expansions in Frataxin Gene oleh Mona ENTEZA­M, Akbar AMIRFIROOZI, Mansoureh TOGHA, Mohammad KERAMATIPOUR

    Diterbitkan 2017-02-01
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  6. 6
    Functional Analysis of A Novel Splicing Mutation in The Mutase Gene of Two Unrelated Pedigrees

    Functional Analysis of A Novel Splicing Mutation in The Mutase Gene of Two Unrelated Pedigrees oleh Somayeh Ahmadloo, Saeed Talebi, Mohammad Miryounesi, Parvin Pasalar, Mohammad Keramatipour

    Diterbitkan 2016-09-01
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  7. 7
    Single Nucleotide Polymorphism rs 2476601 of PTPN22 Gene and Susceptibility to Rheumatoid Arthritis in Iranian Population

    Single Nucleotide Polymorphism rs 2476601 of PTPN22 Gene and Susceptibility to Rheumatoid Arthritis in Iranian Population oleh Somayeh Ahmadloo, Mohsen Taghizadeh, Mohsen Akhiani, Ahmad Salimzadeh, Mohammad Keramatipour

    Diterbitkan 2015-10-01
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  8. 8
    Waardenburg syndrome type 2A in a large Iranian family with a novel MITF gene mutation

    Waardenburg syndrome type 2A in a large Iranian family with a novel MITF gene mutation oleh Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Mohammad Keramatipour, Saeid Morovvati

    Diterbitkan 2021-09-01
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  9. 9
    Investigating the Effect of rs3783605 Single-nucleotide Polymorphism on the Activity of VCAM-1 Promoter in Human Umbilical Vein Endohelial Cells

    Investigating the Effect of rs3783605 Single-nucleotide Polymorphism on the Activity of VCAM-1 Promoter in Human Umbilical Vein Endohelial Cells oleh Fatemeh Dadgar Pakdel, Mohammad Keramatipour, Farshid Noorbakhsh, Saeed Talebi, Mohammad Vodjgani

    Diterbitkan 2015-04-01
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  10. 10
    Once in a Blue Moon, a Very Rare Coexistence of Glutaric Acidemia Type I and Mucopolysaccharidosis Type IIIB in a Patient

    Once in a Blue Moon, a Very Rare Coexistence of Glutaric Acidemia Type I and Mucopolysaccharidosis Type IIIB in a Patient oleh Mohammad Reza Alaei, Meghdad Kheirkhahan, Saeed Talebi, Elham Davoudi-Dehaghani, Mohammad Keramatipour

    Diterbitkan 2020-05-01
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  11. 11
    X-linked SCID with a rare mutation

    X-linked SCID with a rare mutation oleh Fatemeh Sadat Mahdavi, Mohammad Keramatipour, Sarina Ansari, Samin Sharafian, Arezou Karamzade, Marzieh Tavakol

    Diterbitkan 2021-10-01
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  12. 12
    PKD2 mutation in an Iranian autosomal dominant polycystic kidney disease family with misleading linkage analysis data

    PKD2 mutation in an Iranian autosomal dominant polycystic kidney disease family with misleading linkage analysis data oleh Mona Entezam, Mohammad Reza Khatami, Fereshteh Saddadi, Mohsen Ayati, Jamshid Roozbeh, Mohammad Keramatipour

    Diterbitkan 2016-06-01
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  13. 13
    Investigation of the association of G-7A and T-138C single nucleotide polymorphisms on the promoter of MGP gene with renal stone

    Investigation of the association of G-7A and T-138C single nucleotide polymorphisms on the promoter of MGP gene with renal stone oleh Mohammad Keramatipour, Babak Ahadi, Mohsen Taghizadeh, Ali Tabibi, Farshad Zohrabi, Babak Javanmard, Behzad Narouie

    Diterbitkan 2018-05-01
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  14. 14
    Three Novel Variants identified in FBN1 and TGFBR2 in seven Iranian families with suspected Marfan syndrome

    Three Novel Variants identified in FBN1 and TGFBR2 in seven Iranian families with suspected Marfan syndrome oleh Fatemeh Bitarafan, Ehsan Razmara, Mehrnoosh Khodaeian, Mohammad Keramatipour, Alireza Kalhor, Ehsan Jafarinia, Masoud Garshasbi

    Diterbitkan 2020-08-01
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  15. 15
    Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report

    Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report oleh Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Aliagha Alishiri, Mohammad Keramatipour, Zeynab Javanfekr Shahri, Saeid Morovvati

    Diterbitkan 2021-02-01
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  16. 16
    Identification of a Novel Mutation in the PAH Gene in an Iranian Phenylketonuria Family: A Case Report

    Identification of a Novel Mutation in the PAH Gene in an Iranian Phenylketonuria Family: A Case Report oleh Masoumeh RAZIPOUR, Daniz KOOSHAVAR, Elaheh ALAVINEJAD, Seyede Zahra SAJEDI, Neda MOHAJER, Aria SETOODEH, Saeed TALEBI, Mohammad KERAMATIPOUR

    Diterbitkan 2017-04-01
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  17. 17
    Analysis of CFTR Gene Mutations in Children with Cystic Fibrosis, First Report from North-East of Iran

    Analysis of CFTR Gene Mutations in Children with Cystic Fibrosis, First Report from North-East of Iran oleh Atieh Mehdizadeh Hakkak, Mohammad Keramatipour, Saeid Talebi, Azam Brook, Jalil Tavakol Afshari, Amin Raazi, Hamid Reza Kianifar

    Diterbitkan 2013-08-01
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  18. 18
    An Efficient Trio-Based Mini-Haplotyping Method for Genetic Diagnosis of Phenylketonuria

    An Efficient Trio-Based Mini-Haplotyping Method for Genetic Diagnosis of Phenylketonuria oleh Saeed Talebi, Mona Entezam, Neda Mohajer, Golnaz-Ensieh Kazemi-sefat, Masoumeh Razipour, Somayeh Ahmadloo, Aria Setoodeh, Mohammad Keramatipour

    Diterbitkan 2016-07-01
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  19. 19
    The importance of CDC27 in cancer: molecular pathology and clinical aspects

    The importance of CDC27 in cancer: molecular pathology and clinical aspects oleh Golnaz Ensieh Kazemi-Sefat, Mohammad Keramatipour, Saeed Talebi, Kaveh Kavousi, Roya Sajed, Nazanin Atieh Kazemi-Sefat, Kazem Mousavizadeh

    Diterbitkan 2021-03-01
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  20. 20
    CTLA-4 Gene Polymorphisms (-318C/T, +49A/G, +6230A/G) in Iranian Patients with Multiple Sclerosis

    CTLA-4 Gene Polymorphisms (-318C/T, +49A/G, +6230A/G) in Iranian Patients with Multiple Sclerosis oleh Abolfazl Heidari, Mohammad Keramatipour, Ali Akbar Amirzargar, Ali Rashidinezhad, Ahmad Ali Sahmani, Hossein Mozhdehipanah, Mohammad Reza Noori Daloii

    Diterbitkan 2010-12-01
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